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Allyl Barbituric Acid

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Identification
Molecular formula
C11H16N2O4
CAS number
131-29-5
IUPAC name
5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, Allyl Barbituric Acid is in a solid state. It maintains its form as a powder under typical storage and handling conditions.

Melting point (Celsius)
81.00
Melting point (Kelvin)
354.15
Boiling point (Celsius)
90.00
Boiling point (Kelvin)
363.15
General information
Molecular weight
224.25g/mol
Molar mass
224.2530g/mol
Density
1.2600g/cm3
Appearence

Allyl Barbituric Acid typically appears as a white to off-white crystalline powder. It is often supplied in a pure form, where it has a consistent texture and particulate size.

Comment on solubility

Solubility of 5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione

5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione, with its complex structure, presents intriguing characteristics regarding its solubility. Understanding its solubility behavior can provide valuable insights for its application and effectiveness.

Key Solubility Characteristics:

  • Polarity: The presence of hydroxy groups increases polarity, which often enhances solubility in polar solvents like water.
  • Hydrogen Bonding: The potential for hydrogen bonding due to hydroxyl groups can facilitate solvation in solutions.
  • Allyl Group Influence: The allyl substituent may contribute to hydrophobic interactions, affecting solubility in nonpolar solvents.

Moreover, solubility can be influenced by various factors:

  • Temperature: Higher temperatures may increase solubility for solid compounds.
  • pH Levels: Variations in pH can alter the ionization of the compound, impacting solubility.
  • Solvent Composition: A mixture of solvents may enhance overall solubility, particularly in formulations.

In conclusion, while extensive experimental data may be needed to fully characterize solubility in various solvents, it is clear that the unique architecture of 5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione suggests a nuanced solubility profile that can be tailored for specific applications.

Interesting facts

Interesting Facts About 5-Allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione

5-Allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione is a fascinating compound notable for its unique structural features and potential applications. Here are some remarkable facts about this compound:

  • Diverse Functionality: This compound belongs to the pyrimidine family, which is characterized by a six-membered ring containing nitrogen atoms. The incorporation of an allyl group enhances its reactivity and opens doors to various chemical reactions.
  • Hydroxy Group Impact: The presence of a hydroxy group on the cyclohexyl ring contributes to the compound's stability and polarity, making it a potential candidate for biological activities.
  • Biological Relevance: Compounds similar to this have been studied for their therapeutic effects. Their ability to interact with biological systems positions them as candidates for pharmaceutical development.
  • Potential in Organic Synthesis: The unique structural attributes of this compound provide opportunities for innovative synthetic pathways, particularly in the creation of complex organic molecules.

An exciting quote in the field of chemistry states, "Chemistry is the central science; it connects physics with other natural sciences such as geology and biology." This compound exemplifies that connection, bridging synthetic chemistry with potential biological applications.

As research advances, compounds like 5-allyl-1-(4-hydroxycyclohexyl)hexahydropyrimidine-2,4,6-trione may unveil new horizons in both materials science and medicinal chemistry, underscoring the ever-evolving landscape of chemical discovery.

Synonyms
5-Allyl-1-(4-hydroxycyclohexyl)barbituric acid
4256-27-3
BRN 0758624
BARBITURIC ACID, 5-ALLYL-1-(4-HYDROXYCYCLOHEXYL)-
DTXSID60962559
6-Hydroxy-3-(4-hydroxycyclohexyl)-5-(prop-2-en-1-yl)pyrimidine-2,4(3H,5H)-dione